PED CERTIFICATION - PRESSURE EQUIPMENT DIRECTIVE
What is PED Certification?
The Pressure Equipment Directive (PED) is European Legislation aimed at removing the technical barriers to trade relating to the supply of pressure equipment throughout Europe. The PED is based on Essential Safety Requirements (ESRs) that govern design, manufacturing, inspection, and testing.
PED affects most equipment that will be placed on the market in the European Economic Area (EEA) designed for pressures above 0.5 bar g or 7.25 psi g.
The European directives for pressure equipment consist of:
- Simple pressure vessels (SPVD) – 2014/29/EU: Vessels for compressed air and nitrogen. For example, air compressors, pneumatic systems, braking systems, etc.
- Pressure equipment (PED) – 2014/68/EU:: Pressure vessels, heat exchangers, reactors, cryogenic vessels, water tube boilers, shell boilers, safety valves, valves, fire extinguishers, cylinders for breathing apparatus, etc.
- Transportable pressure equipment (TPED) – 2010/35/EU: High-pressure gas cylinders, LPG cylinders, cryogenic transport vessels, one-way bottles, gas cartridges, bundles of cylinders (frames), tanks for the transport of gases (cryogenic gases/LPG/etc.) on road and rail.
Benefits of PED Certification
Facilitate continual improvement
Product Reliability
Reputation of the company increases
Increase market opportunities
Keeps You Unique
Continual Business Improvements
Who can be certified PED Certification?
The PED offers manufacturers of pressure equipment 14 different conformity assessment options which permit the pressure equipment manufacturer to demonstrate compliance by variants on Quality Assurance.
Pressure Vessels
Piping
Steam Generators
Pressure Accessories
Safety Accessories
Steam Boilers
Document required for PED Certification
- Technical File, Product Master File (TCF)
- Product Testing
- System Manual
- System Procedure
- Policy
- Objectives
- Mission & Vision
- Plant Master File
- Standard Operating Procedure (SOP)
- Checklist
- Forms
- Formats
- Records
The extent of Documented Information differs as per:
- Product and it's uses
- Testing requirement of products
- Directive in which product classified
- Self Certification or Compliance Certification
- Notify body Certificate
Role of Shamkris and Process of PED Certification
Shamkris adopts a results-oriented approach to compliance product certification, A simple & practical method of product certification organization in timely compliance and fulfills the product certification requirement. Shamkris support 100% on documentation required to comply with product certification either by self-certification or notify body certification to depend on directives.
The implementation process is described below:
Time Frame
Task
Process
Day 1
Scope defined
Self Certification/NoBo
Selection
Cost Estimates
- Finding directive and EN standard applicable to the product
- Selecting the appropriate certification scheme
- Based on the scope of the product and certification scheme
Week 1
Developing Documents
- Technical file, Plant Master file and Test Protocol
- Management System Manual, Management System Procedures, Policy, Objectives, Forms etc.
- Review of Standard Operating Procedures (SOP)
Week 4
Implementing Product Management System
- PED Awareness training to QC manager and Production Manager
- Implementing a well-documented manual throughout the life cycle of the product
Week 8
Internal Audit
MRM
CAPA
- Internal audits identifying nonconformities related to PED requirements
- Management Review Meetings
- Corrective and Preventive Action plan for nonconformities
Week 10
Self Certification/NoBo
Audit
N-C Closing
- Shamkris acts on your behalf and assists you in the third-party audit
- Closing of any nonconformities identified by the Self Certification/NoBo
Week 12
Self Certification/NoBo
- PED certificates issued for 5 years
- Surveillance Audits yearly
- If PED is issued for customize project then their is no Validity.
Year on Year
Yearly Compliance
- Support of Yearly documentation for audit